Pantoprazole Sodium Tablet, Delayed Release
NDC Package 51655-075-52
Package Information
Pantoprazole Sodium tablets is pantoprazole is used to treat certain stomach and esophagus problems (such as acid reflux). This formulation utilizes a tablet, delayed release delivery system. Marketed by Northwind Health Company, Llc, this product is identified by NDC 51655-075 and is authorized under FDA application ANDA202038.
Identification & Billing
- RxCUI: 251872 - pantoprazole sodium 20 MG Delayed Release Oral Tablet
- RxCUI: 251872 - pantoprazole 20 MG Delayed Release Oral Tablet
- RxCUI: 251872 - pantoprazole 20 MG (as pantoprazole sodium sesquihydrate 22.56 MG) Delayed Release Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 51655 - Northwind Health Company, Llc
- 51655-075 - Pantoprazole Sodium
- 51655-075-52 - 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
- 51655-075 - Pantoprazole Sodium
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (51655-075). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 51655-075-52 identifies a specific commercial package of 30 tablet, delayed release in 1 bottle, plastic of Pantoprazole Sodium, a human prescription drug labeled by Northwind Health Company, Llc. This tablet, delayed release is formulated for oral use and contains pantoprazole sodium as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Northwind Health Company, Llc on September 27, 2022. The current certification is valid through December 31, 2027.
What are the primary indications for this medication?
Pantoprazole is used to treat certain stomach and esophagus problems (such as acid reflux). It works by decreasing the amount of acid your stomach makes. This medication relieves symptoms such as heartburn, difficulty swallowing, and persistent cough. It helps heal acid damage to the stomach and esophagus, helps prevent ulcers, and may help prevent cancer of the esophagus. Pantoprazole belongs to a class of drugs known as proton pump inhibitors (PPIs).
How is this Northwind Health Company, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 51655007552. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.